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- Mary Jane Gore
Extract
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FDA APPROVALS The U.S. Food and Drug Administration has approved the first rapid assay screening test that physicians can use in their offices to help diagnose patients with bladder cancer. The FDA approved Matritech's NMP22® BladderChek™ test, which detects a bladder cancer nuclear matrix protein in urine of patients. Contact (617) 928-0820, ext. 248, or visit www.matritech.com.
NEW PRODUCTS Tecan US has announced a strategic alliance with GE Medical Systems for Tecan's front-end Genesis FE500 Workcell. Together, the two companies plan to enhance clinical diagnostics lab output using Tecan's state-of-the-art robotic equipment to enhance sample flow, coupled by world-class customer service by GE Medical Systems. As a modular, compact front-end automation workcell, the Genesis FE500 combines all pre-analytical functions including pre-sorting, centrifugation, volume check and clot detection, decapping, secondary tube labeling, aliquotting and destination sorting into analyzer racks from a variety of manufacturers. Contact GE Medical Systems Britt Zarling, at (262) 544-3453.
Leica Microsystems introduces the…
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